Medical Device Services
Medical Device
ND Global’s services serve as a pillar of strength for organizations aiming for operational excellence, regulatory compliance, and the delivery of products that uphold the highest standards. We are committed to making the registration process hassle-free, paving the way for your success in a global landscape. Our team is committed to provide you service which will suit your needs.
Regulatory Services
We at ND Global have great experience in global regulations (EU-MDR, USFDA, Health Canada, Swiss Medic, and more). We have dedicated team who can help you in CER, Risk Management, PMS, Technical Files, Gap Analysis, UDI & IFU preparation. Learn More
Quality Services
ND Global can help you in Robust QMS such compliance, and continuous enhancement. We have tailored support for FDA QSR, EU MDR, ISO standards which customized as per your requirements.Learn More
End-to-end Product Development
ND Global adheres to ISO 13485 & FDA Excellence. We have custom solutions such as market-aligned, user-focused as we use holistic approach which include tech, clinical, commercial, legal, and early risk mitigation. Learn More
